Canonical Allele Identifier: CA1172961673
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1667514966

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009216_67009218del , CM000663.2:g.67009216_67009218del GRCh38
NC_000001.10:g.67474899_67474901del , CM000663.1:g.67474899_67474901del GRCh37
NC_000001.9:g.67247487_67247489del NCBI36
NG_012933.1:g.50183_50185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-48_877-46del MANE Select ENSP00000235345.5:n.877-48_877-46del
ENST00000235345.5:c.877-48_877-46del ENSP00000235345.5:n.877-48_877-46del
NM_015139.2:c.877-48_877-46del NP_055954.1:n.877-48_877-46del
XM_006710478.1:c.958-48_958-46del XP_006710541.1:n.958-48_958-46del
XM_011541070.1:c.958-48_958-46del XP_011539372.1:n.958-48_958-46del
XM_006710478.2:c.958-48_958-46del XP_006710541.1:n.958-48_958-46del
XM_011541070.2:c.958-48_958-46del XP_011539372.1:n.958-48_958-46del
XR_001737057.2:n.1461-48_1461-46del
XR_001737058.2:n.2246-48_2246-46del
NM_015139.3:c.877-48_877-46del MANE Select NP_055954.1:n.877-48_877-46del